posted on 2024-08-20, 11:04authored byYuanyuan He, Laurent Rémusat, Marceau Lecasble, Jean-Christophe Viennet, Isis Criouet, David Boulesteix, Nadezda Khodorova, Ludovic Delbes, Maxime Guillaumet, François Baudin, Boris Laurent, Arnaud Buch, Sylvain Bernard
Nucleobases such as guanine, xanthine, and uracil have
been detected
in numerous carbonaceous chondrites (CCs), with isotope signatures
indicating their extraterrestrial origin. A correlation between nucleobase
concentrations and the alteration degree of parent bodies is often
reported, highlighting the importance of understanding the influence
of aqueous alteration on nucleobase evolution to decode early solar
system organic materials. Therefore, a laboratory investigation of
the evolution of guanine, uracil, and xanthine was performed under
aqueous alteration conditions typical of CCs. Given the intimate association
of organic molecules with inorganic materials in CC matrices, we also
included a set of inorganic phases in this study to discuss the influence
of minerals on nucleobase evolution during aqueous alteration. Results
showed that guanine and uracil exhibit high stability, while xanthine
undergoes decarboxylation. Saponite traps about 25% of xanthine, 53%
of uracil, and nearly all guanine, promoting nucleobase preservation.
The isotope values (δ13C and δ15N) of nucleobases remained constant through aqueous alteration, suggesting
that their isotope signatures are related to synthesis in cold environments
in the proto solar nebula or the parent molecular cloud. The relative
stability of guanine during aqueous alteration explains its abundance
in meteorites. Nevertheless, other processes such as (geo)chromatographic
effects may account for the observed decrease in guanine abundance
with the increasing degree of alteration in CCs. The reported concentrations
of uracil and xanthine in CCs are not correlated with the alteration
degree; hence, differences in relative abundance are either related
to different parent body reservoirs or synthesis/migration during
aqueous alteration events.